Production of broad molecular weight polyethylene

ABSTRACT

Broad molecular weight polyethylene and polyethylene having a bimodal molecular weight profile can be produced with chromium oxide based catalyst systems employing alkyl silanols. The systems may also contain various organoaluminum compounds. Catalyst activity and molecular weight of the resulting polyethylene may also be tuned using the present invention.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation of Ser. No. 11/343,538, filed Jan.31, 2006, now allowed, which is a divisional of Ser. No. 10/762,494,filed Jan. 22, 2004, now abandoned, which claims the benefit of Ser. No.60/450,395, filed Feb. 26, 2003, the disclosures of which areincorporated by reference.

TECHNICAL FIELD

The present invention relates to the use of chromium-based catalystswith alkyl silanols such as triphenyl silanol with or without aluminumalkyl activators. The use of aluminum alkyls and alkyl silanols allowsfor the control of polymer molecular weight and molecular weightdistribution and results in a catalyst with behavior similar tosilylchromate on silica catalyst. Bimodal polyethylene may be producedwith the present invention.

BACKGROUND OF THE INVENTION

Ethylene polymers have been used generally and widely as resin materialsfor various molded articles and are required to have differentproperties depending on the molding method and purpose. For example,polymers having relatively low molecular weights and narrow molecularweight distributions are suitable for articles molded by an injectionmolding method. On the other hand, polymers having relatively highmolecular weights and broad molecular weight distributions are suitablefor articles molded by blow molding or inflation molding. In manyapplications, medium-to-high molecular weight polyethylenes aredesirable. Such polyethylenes have sufficient strength for applicationswhich call for such strength (e.g., pipe applications), andsimultaneously possess good processability characteristics.

Ethylene polymers having broad molecular weight distributions can beobtained by use of a chromium catalyst obtained by calcining a chromiumcompound carried on an inorganic oxide carrier in a non-reducingatmosphere to activate it such that at least a portion of the carriedchromium atoms is converted to hexavalent chromium atoms (Cr+6). This iscommonly referred to in the art as the Phillips catalyst. The respectivematerial is impregnated onto silica, fluidized and heated in thepresence of oxygen to about 400° C.-860° C., converting chromium fromthe +3 oxidation state to the +6 oxidation state. A second chromiumcatalyst used for high density polyethylene applications consists ofsilylchromate (bis-triphenylsilyl chromate) absorbed on dehydratedsilica and subsequently reduced with diethylaluminum ethoxide (DEALE).The resulting polyethylenes produced by each of these catalysts aredifferent in some important properties. Chromium oxide-on-silicacatalysts have good productivity (g PE/g catalyst), also measured byactivity (g PE/g catalyst-hr) but produce polyethylenes with molecularweight distributions lower than that desired for certain applications.Silylchromate-based catalysts produce polyethylenes with desirablemolecular weight distribution characteristics (broader molecular weightdistribution with a high molecular weight shoulder on molecular weightdistribution curve, indicative of two distinct molecular weightpopulations).

Monoi, in Japanese Patent 200202412 discloses the use of inorganicoxide-supported Cr+6-containing solid components (A) prepared bysintering under nonreducing conditions, dialkylaluminum functionalgroup-containing alkoxides (B), and trialkylaluminum (C). The resultingethylene polymers are said to possess good environmental stress crackresistance and good blow molding creep resistance. U.S. Application2002042428 discloses a method of ethylene polymerization in co-presenceof hydrogen using a trialkylaluminum compound-carried chromium catalyst(A), wherein the chromium catalyst is obtained by calcination-activatinga Cr compound carried on an inorganic oxide carrier in a non-reducingatmospheric to convert Cr atoms into the hexavalent state and thentreating A with a trialkylaluminum compound in an inert hydrocarbonsolvent and removing the solvent in a short time.

Hasebe et al. Japanese Patent 2001294612 discloses catalysts containinginorganic oxide-supported Cr compounds calcined at 300° C.-1100° C. in anonreducing atmosphere, R_(3-n)AlL_(n) (R=C1-12 alkyl; L=C1-8 alkoxy,phenoxy; 0≦n≦1), and Lewis base organic compounds. The catalysts aresaid to produce polyolefins with high molecular weight and narrowmolecular weight distribution.

Hasebe et al., in Japanese Patent 2001198811 discloses polymerization ofolefins using catalysts containing Cr oxides (supported on fireresistant compounds and activated by heating under nonreductiveconditions) and R_(3-n)AlL_(n) (R=C1-6 alkyl; L=C1-8 alkoxy, phenoxy;n>0.5 but <1). Ethylene is polymerized in the presence of SiO₂-supportedCrO₃ and a reaction product of a 0.9:1 MeOH-Et₃Al mixture to give apolymer with melt index 0.18 g/10 min at 190° C. under 2.16-kg load and1-hexene content 1.6 mg/g-polymer.

Da et al, in Chinese Patent 1214344 teaches a supported chromium-basedcatalyst for gas-phase polymerization of ethylene prepared byimpregnating an inorganic oxide support having hydroxyl group on thesurface with an inorganic chromium compound aqueous solution; drying inair; activating the particles in oxygen; and reducing the activatedcatalyst intermediate with an organic aluminum compound. 10 g commercialsilica gel was mixed with 0.05 mol/L CrO₃ aqueous solution, dried at80-120° C. for 12 h, baked at 200° C. for 2 h and 600° C. for 4 h,reduced with 25% hexane solution of diethylethoxyaluminum to give powdercatalyst with Cr content 0.25% and Al/Cr ratio of 3.

Durand et al, U.S. Pat. No. 5,075,395, teaches a process for eliminationof the induction period in the polymerization of ethylene by bringingethylene in contact under fluidized-bed polymerization conditions and/orstirred mechanically, with a charge powder in the presence of a catalystcomprising a chromium oxide compound associated with a granular supportand activated by thermal treatment, this catalyst being used in the formof a prepolymer. The Durand process is characterized in that the chargepowder employed is previously subjected to a treatment by contacting thesaid charge powder with an organoaluminum compound, in such a way thatthe polymerization starts up immediately after the contacting of theethylene with the charge powder in the presence of the prepolymer.

McDaniel, in U.S. Pat. No. 4,559,394 teaches the polymerization ofolefins using activated chromium catalysts and tertiary alcohols. Thesepatents teach the addition of alcohols to chromium oxide to improvechromium distribution. McDaniel adds the tertiary alcohol prior tocatalyst activation. Interestingly, McDaniel teaches that silanols donot work to achieve this end.

U.S. Pat. Nos. 4,454,242 and 4,451,573 to Ikegami et al, employ silanolsin conjunction with chromium oxide catalysts treated with zirconium ortitanium and alkylmagnesium compounds to make improved environmentalstress crack resistance (ESCR) products.

Chromium catalysts based on chromocene and silanols have been preparedand deposited on silica to increase catalyst activity as taught in U.S.Pat. No. 4,153,576 to Karol et al. U.S. Pat. Nos. 3,767,635; 3,629,216;and 3,759,918, assigned to Mitsubishi Chemical Industries, Ltd., teachthe addition of pentaalkylsiloxyalanes to supported chromium oxidecatalysts to make useful polyethylenes.

Chromium oxide (CrOx) based catalysts have high activity with moderateinduction times and produce polymers with high molecular weights andintermediate molecular weight distributions. Silylchromate-basedcatalysts have poorer activity, but produce polymers with a broadermolecular weight distribution. Silylchromate catalysts are typicallymore costly than chromium oxide catalysts. It would be desirable to havea method that allows for the tuning of chromium oxide based catalystssuch that the polymers produced by them approach the characteristics ofpolymers produced using silylchromate-based catalysts. For backgroundinformation regarding silylchromate catalysis, see e.g., U.S. Pat. Nos.3,324,095 and 3,324,101 to Carrick et al. The prior art lacks aninexpensive, facile method for modifying a chromium oxide catalyst suchthat polymer produced by it can be variably tuned to approach polymerproduced by silylchromate-based catalyst systems. Additionally, theprior art is devoid of any teaching of the use of silanols in atwo-catalyst system to obtain polymers with bimodal molecular weightdistribution profiles.

While the prior art contains these and other examples of the use ofmodified Phillips-type catalysts, there has not yet been disclosed amethod for the control of molecular weight distribution. The presentinvention provides a method for the production of polyethylenecharacterized by the control of both the molecular weight and thebreadth of molecular weight distribution. The present invention alsoprovides a method to produce a bimodal polyethylene through the use oftwo chromium-based catalyst systems.

SUMMARY OF THE INVENTION

The present invention is directed to a system and method for thepolymerization ethylene using chromium-based catalysts with control ofmolecular weight and molecular weight distribution. It also provides forthe production of bimodal polyethylene through the use of catalystsystems having two chrome catalysts.

In one aspect of the present invention, there is a supported chromiumcatalyst comprising chromium oxide, a silica-containing supportcomprising silica selected from the group consisting of silica having(a) a pore volume of about 1.1-1.8 cm³/g and a surface area of about245-375 m²/g, (b) a pore volume of about 2.4-3.7 cm³/g and a surfacearea of about 410-620 m²/g, and (c) a pore volume of about 0.9-1.4 cm³/gand a surface area of about 390-590 m²/g, and an alkyl silanol, whereinthe supported chromium catalyst is activated at 400-860° C., prior tothe addition of said alkyl silanol.

In another embodiment, the catalyst further comprises titaniumtetraisopropoxide. In another embodiment, the catalyst further comprisesan organoaluminum compound. In a specific embodiment having anorganoaluminum compound, the activated chromium catalyst is treatedfirst with the alkyl silanol and then with the organoaluminum compound.In another specific embodiment having an organoaluminum compound, thesilica has a pore volume of about 2.4-3.7 cm³/g and a surface area ofabout 410-620 m²/g and said organoaluminum compound is an alkyl aluminumalkoxide compound. In yet another specific embodiment having anorganoaluminum compound, the silica has a pore volume of about 1.1-1.8cm³/g and a surface area of about 245-375 m²/g, and said organoaluminumcompound is an alkyl aluminum alkoxide compound. In another specificembodiment having an organoaluminum compound, the organoaluminumcompound is added in-situ. In yet another specific embodiment having anorganoaluminum compound, the catalyst further comprises at least asecond chromium-based compound. In a specific embodiment having at leasta second chromium-based compound, the second chromium-based compound isa chromium oxide on silica or an organoaluminum-d reduced chromium oxideon silica.

In another embodiment of the catalyst having an organoaluminum compound,the alkyl silanol or the organoaluminum compound or both the alkylsilanol and the organoaluminum compound are added in-situ. In a specificembodiment, the alkyl silanol and the organoaluminum compound arepre-mixed prior to said in-situ addition.

In another embodiment of the catalyst having an organoaluminum compound,the organoaluminum compound is an alkyl aluminum alkoxide compound. In aspecific embodiment, the alkyl aluminum alkoxide compound is diethylaluminum ethoxide. In another specific embodiment, the catalyst havingan alkyl aluminum alkoxide compound is formed by the in situ addition ofsaid alkyl aluminum alkoxide compound. In a specific embodiment, thealkyl aluminum alkoxide compound is diethyl aluminum ethoxide.

In another embodiment of the catalyst having an organoaluminum compound,the organoaluminum compound is an alkyl aluminum compound. In a specificembodiment, the alkyl aluminum compound is selected from the groupconsisting of triethyl aluminum, tri-isobutyl aluminum, and tri-n-hexylaluminum. In another specific embodiment, the catalyst is formed by thein situ addition of the alkyl aluminum compound. In yet another specificembodiment, the alkyl aluminum compound added in-situ is tri-isobutylaluminum.

In another embodiment of the supported chromium catalyst, the catalystis activated at 600-860° C. In another embodiment of the supportedchromium catalyst, the alkyl silanol is triphenyl silanol.

In the present invention, there is also a supported chromium catalystcomprising chromium oxide, a silica-containing support comprising silicaselected from the group consisting of silica having (a) a pore volume ofabout 1.1-1.8 cm³/g and a surface area of about 245-375 m²/g, (b) a porevolume of about 2.4-3.7 cm³/g and a surface area of about 410-620 m²/g,and (c) a pore volume of about 0.9-1.4 cm³/g and a surface area of about390-590 m²/g and, an organoaluminum compound, wherein the supportedchromium catalyst is activated at 400-860° C.

In a specific embodiment, the organoaluminum compound is diethylaluminum triethylsiloxide. In another embodiment, the catalyst furthercomprises titanium tetraisopropoxide.

Also in the present invention, there is a supported chromium catalystcomprising chromium oxide, a silica-containing support comprising silicaselected from the group consisting of silica having (a) a pore volume ofabout 1.1-1.8 cm³/g and a surface area of about 245-375 m²/g, (b) a porevolume of about 2.4-3.7 cm³/g and a surface area of about 410-620 m²/g,and (c) a pore volume of about 0.9-1.4 cm³/g and a surface area of about390-590 m²/g wherein said supported chromium catalyst is activated at400-860° C., and, a second chromium-based compound comprisingsilylchromate on silica treated with an organoaluminum compound. In aspecific embodiment, the chromium oxide catalyst component is treatedwith an organoaluminum compound after activation. In another embodiment,the catalyst further comprises titanium tetraisopropoxide.

In the present invention, there is also a process for producing anethylene polymer comprising the steps of contacting ethylene underpolymerization conditions with a catalyst system, said catalyst systemcomprising chromium oxide, an alkyl silanol compound, and asilica-containing support comprising silica selected from the groupconsisting of silica having (a) a pore volume of about 1.1-1.8 cm³/g anda surface area of about 245-375 m²/g, (b) a pore volume of about 2.4-3.7cm³/g and a surface area of about 410-620 m²/g, and (c) a pore volume ofabout 0.9-1.4 cm³/g and a surface area of about 390-590 m²/g and,controlling one or more of catalyst activity, polymer Mz/Mw, polymerMw/Mn, and polymer density of the resulting ethylene polymer by varyingthe level of addition of said alkyl silanol.

In one embodiment of the process the polymer Mw/Mn is controlled togreater than about 15 and the polymer Mz/Mw is controlled to greaterthan about 5. In another embodiment of the process, the catalyst systemfurther comprises an organoaluminum compound. In a specific embodimentof the process where the catalyst system further comprisesorganoaluminum, the catalyst system further comprises at least a secondchromium-based catalyst. In a specific embodiment of the process wherethe catalyst system further comprises a second chromium-based catalyst,the second chromium-based compound is a chromium oxide on silica or anorganoaluminum-reduced chromium oxide on silica. In another specificembodiment of the process where the catalyst system further comprises asecond chromium-based catalyst, the organoaluminum compound is an alkylaluminum alkoxide. In another embodiment wherein the organoaluminumcompound is an alkyl aluminum alkoxide, the alkyl aluminum alkoxide isdiethylaluminum ethoxide. In another embodiment, the organoaluminumcompound is an alkyl aluminum compound. In another embodiment of theprocess using alkyl aluminum compound, the alkyl aluminum compound isselected from the group consisting of triethyl aluminum, tri-isobutylaluminum, and tri-n-hexyl aluminum. In another embodiment of theprocess, the catalyst system further comprises titaniumtetraisopropoxide.

In another embodiment, there is a process for producing an ethylenepolymer comprising the steps of contacting ethylene under polymerizationconditions with a catalyst system, said catalyst system comprisingchromium oxide, a silica-containing support comprising silica selectedfrom the group consisting of silica having (a) a pore volume of about1.1-1.8 cm³/g and a surface area of about 245-375 m²/g, (b) a porevolume of about 2.4-3.7 cm³/g and a surface area of about 410-620 m²/g,and (c) a pore volume of about 0.9-1.4 cm³/g and a surface area of about390-590 m²/g wherein the supported chromium catalyst is activated at400-860° C. and, a second chromium-based compound comprisingsilylchromate on silica treated with an organoaluminum compound and,controlling one or more of polymer molecular weight, polymer Mz/Mw,polymer Mw/Mn, and distribution of comonomer incorporation by varyingthe relative amount of each of the chromium oxide and the secondchromium-based compound. In another embodiment of the process thechromium oxide catalyst component is treated with an organoaluminumcompound after activation. In another embodiment, the catalyst systemfurther comprises titanium tetraisopropoxide.

There is also an ethylene polymer having a density of 0.918-0.970 g/cm³and a flow index (I21) of 1-500 and produced by the process comprisingthe steps of contacting ethylene under polymerization conditions with acatalyst system, the catalyst system comprising chromium oxide, an alkylsilanol compound, and a silica-containing support comprising silicaselected from the group consisting of silica having (a) a pore volume ofabout 1.1-1.8 cm³/g and a surface area of about 245-375 m²/g, (b) a porevolume of about 2.4-3.7 cm³/g and a surface area of about 410-620 m²/g,and (c) a pore volume of about 0.9-1.4 cm³/g and a surface area of about390-590 m²/g; and, controlling one or more of catalyst activity, polymerMz/Mw, polymer Mw/Mn, and polymer density of the resulting ethylenepolymer by varying the level of addition of the alkyl silanol.

In another embodiment, there is an ethylene polymer having a density of0.918-0.970 g/cm³ and a flow index (I21) of 1-500 and produced by theprocess comprising the steps of contacting ethylene under polymerizationconditions with a catalyst system, the catalyst system comprisingchromium oxide, an alkyl silanol compound, an organoaluminum compound,and a silica-containing support comprising silica selected from thegroup consisting of silica having (a) a pore volume of about 1.1-1.8cm³/g and a surface area of about 245-375 m²/g, (b) a pore volume ofabout 2.4-3.7 cm³/g and a surface area of about 410-620 m²/g, and (c) apore volume of about 0.9-1.4 cm³/g and a surface area of about 390-590m²/g; and, controlling one or more of catalyst activity, polymer Mz/Mw,polymer Mw/Mn, and polymer density of the resulting ethylene polymer byvarying the level of addition of the alkyl silanol.

In another embodiment, there is an ethylene polymer having a density of0.918-0.970 g/cm³ and a flow index (I21) of 1-500 and produced by theprocess comprising the steps of contacting ethylene under polymerizationconditions with a catalyst system, the catalyst system comprisingchromium oxide, an alkyl silanol compound, an organoaluminum compound,at least a second chromium-based catalyst, and a silica-containingsupport comprising silica selected from the group consisting of silicahaving (a) a pore volume of about 1.1-1.8 cm³/g and a surface area ofabout 245-375 m²/g, (b) a pore volume of about 2.4-3.7 cm³/g and asurface area of about 410-620 m²/g, and (c) a pore volume of about0.9-1.4 cm³/g and a surface area of about 390-590 m²/g; and, controllingone or more of catalyst activity, polymer Mz/Mw, polymer Mw/Mn, andpolymer density of the resulting ethylene polymer by varying the levelof addition of the alkyl silanol.

In another embodiment, there is an ethylene polymer having a density of0.918-0.970 g/cm³ and a flow index (I21) of 1-500 and produced by theprocess comprising the steps of contacting ethylene under polymerizationconditions with a catalyst system, the catalyst system comprisingchromium oxide, an alkyl silanol compound, an organoaluminum compound,at least a second chromium-based catalyst wherein the secondchromium-based catalyst is a chromium oxide on silica or anorganoaluminum-reduced chromium oxide on silica, and a silica-containingsupport comprising silica selected from the group consisting of silicahaving (a) a pore volume of about 1.1-1.8 cm³/g and a surface area ofabout 245-375 m²/g, (b) a pore volume of about 2.4-3.7 cm³/g and asurface area of about 410-620 m²/g, and (c) a pore volume of about0.9-1.4 cm³/g and a surface area of about 390-590 m²/g; and, controllingone or more of catalyst activity, polymer Mz/Mw, polymer Mw/Mn, andpolymer density of the resulting ethylene polymer by varying the levelof addition of the alkyl silanol.

In another embodiment, there is an ethylene polymer having a density of0.918-0.970 g/cm³ and a flow index (I21) of 1-500 and produced by theprocess comprising the steps of contacting ethylene under polymerizationconditions with a catalyst system, said catalyst system comprisingchromium oxide, a silica-containing support comprising silica selectedfrom the group consisting of silica having (a) a pore volume of about1.1-1.8 cm³/g and a surface area of about 245-375 m²/g, (b) a porevolume of about 2.4-3.7 cm³/g and a surface area of about 410-620 m²/g,and (c) a pore volume of about 0.9-1.4 cm³/g and a surface area of about390-590 m²/g wherein said supported chromium catalyst is activated at400-860° C.; wherein the chromium oxide catalyst component is treatedwith an organoaluminum compound after activation and, a secondchromium-based compound comprising silylchromate on silica treated withan organoaluminum compound and, controlling one or more of polymermolecular weight, polymer Mz/Mw, polymer Mw/Mn, and distribution ofcomonomer incorporation by varying the relative amount of each of saidchromium oxide and said second chromium-based compound.

The foregoing has outlined rather broadly the features and technicaladvantages of the present invention in order that the detaileddescription of the invention that follows may be better understood.Additional features and advantages of the invention will be describedhereinafter which form the subject of the claims of the invention. Itshould be appreciated by those skilled in the art that the conceptionand specific embodiment disclosed may be readily utilized as a basis formodifying or designing other structures for carrying out the samepurposes of the present invention. It should also be realized by thoseskilled in the art that such equivalent constructions do not depart fromthe spirit and scope of the invention as set forth in the appendedclaims. The novel features which are believed to be characteristic ofthe invention, both as to its organization and method of operation,together with further objects and advantages will be better understoodfrom the following description when considered in connection with theaccompanying figures. It is to be expressly understood, however, thateach of the figures is provided for the purpose of illustration anddescription only and is not intended as a definition of the limits ofthe present invention.

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the present invention, reference isnow made to the following descriptions taken in conjunction with theaccompanying drawing, in which:

FIG. 1. Possible structure of chromium oxide-on-silica (“Phillips”)catalyst.

FIG. 2. Possible structure of silylchromate-on-silica catalyst.

FIG. 3. Effect of TPS on CrOx catalysts kinetic profile.

FIG. 4. Effect of TPS on CrOx catalyst polymer molecular weightdistribution.

FIG. 5. Effect of TPS on CrOx catalyst kinetic profile; 5A, CrOx; 5B,Ti—CrOx.

FIG. 6. Effect of TES on CrOx catalyst kinetic profile.

FIG. 7. Kinetic profile of CrOx catalyst treated with TPS and DEALE.

FIG. 8. Effect of DEALSi on CrOx catalyst kinetic profile.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, “a” or “an” is defined herein as one or more.

As used herein, “in situ,” in reference to the mode of addition of acomponent to the catalyst, is defined herein as addition to the catalystin the reactor. Therefore, when a catalyst component is added in situ,it is added to the remaining catalyst components in the reactor and isnot combined with the other catalyst components prior to their transportto the reactor. “In reactor” is synonymous with and used interchangeablyherein with “in situ.”

As used herein, “in catalyst” or “on catalyst,” in reference to the modeof addition of a component to the catalyst, is defined herein asaddition directly to the catalyst prior to introduction of the catalystto the reactor. Therefore, when a component is added to the catalyst “incatalyst” or “on catalyst,” it is added to the other catalyst componentsprior to the transport of the aggregate to the reactor.

As used herein, the term alkyl aluminum is defined as a compound havingthe general formula R₃Al wherein R can be any of one to twelve carbonalkyl or aryl groups. The R groups can be the same or different.

As used herein, the term alkyl aluminum alkoxide is defined as acompound having the general formula R₂—Al—OR wherein R can be any of oneto twelve carbon alkyl groups and OR is a one to twelve carbon alkoxy orphenoxy group. The R groups can be the same or different.

As used herein, the term “alkyl silanol” is defined as a compound havingthe general formula R₃—Si—OH where R can be any of one to twelve carbonalkyl groups or aryl groups. The R groups can be the same or different.

As used herein, “DEALE” means diethyl aluminum ethoxide.

As used herein, “DEALSi” means diethylaluminum triethylsiloxide and isused to represent the reaction product of TEAL and triethylsilanol.

As used herein, “TEA1” means triethyl aluminum.

As used herein, “TES” means triethylsilanol.

As used herein, “TIBA” means tri-isobutyl aluminum.

As used herein, “TPS” means triphenylsilanol.

As used herein, “TTIP” means titanium tetraisopropoxide.

As used herein, “M_(w)” is the weight-average molecular weight.

As used herein, “M_(n)” is the number-average molecular weight.

As used herein, “M_(z)” is the z-average molecular weight.

As used herein, “molecular weight distribution” is equal to M_(w)/M_(n).

The invention is applicable to the polymerization of olefins by anysuspension, solution, slurry, or gas phase process, using knownequipment and reaction conditions, and is not limited to any specifictype of polymerization system. Generally, olefin polymerizationtemperatures range from about 0° C. to about 300° C. at atmospheric,subatmospheric, or superatmospheric pressures. Slurry or solutionpolymerization systems may utilize subatmospheric or superatmosphericpressures and temperatures in the range of about 40° C. to about 300° C.A useful liquid phase polymerization system is described in U.S. Pat.No. 3,324,095. Liquid phase polymerization systems generally comprise areactor to which olefin monomer and catalyst composition are added, andwhich contains a liquid reaction medium for dissolving or suspending thepolyolefin. The liquid reaction medium may consist of the bulk liquidmonomer or an inert liquid hydrocarbon that is nonreactive under thepolymerization conditions employed. Although such an inert liquidhydrocarbon need not function as a solvent for the catalyst compositionor the polymer obtained by the process, it usually serves as solvent forthe monomers employed in the polymerization. Among the inert liquidhydrocarbons suitable for this purpose are isobutane, isopentane,hexane, cyclohexane, heptane, benzene, toluene, and the like. Reactivecontact between the olefin monomer and the catalyst composition shouldbe maintained by constant stirring or agitation. The reaction mediumcontaining the olefin polymer product and unreacted olefin monomer iswithdrawn from the reactor continuously. The olefin polymer product isseparated, and the unreacted olefin monomer and liquid reaction mediumare recycled into the reactor.

The invention is, however, especially useful with gas phasepolymerization systems, with superatmospheric pressures in the range of1 to 1000 psi, preferably 50 to 400 psi, most preferably 100 to 300 psi,and temperatures in the range of 30 to 130° C., preferably 65 to 110° C.Stirred or fluidized bed gas phase polymerization systems areparticularly useful. Generally, a conventional gas phase, fluidized bedprocess is conducted by passing a stream containing one or more olefinmonomers continuously through a fluidized bed reactor under reactionconditions and in the presence of catalyst composition at a velocitysufficient to maintain a bed of solid particles in a suspendedcondition. A stream containing unreacted monomer is withdrawn from thereactor continuously, compressed, cooled, optionally partially or fullycondensed, and recycled into the reactor. Product is withdrawn from thereactor and make-up monomer is added to the recycle stream. As desiredfor temperature control of the polymerization system, any gas inert tothe catalyst composition and reactants may also be present in the gasstream. In addition, a fluidization aid such as carbon black, silica,clay, or talc may be used, as disclosed in U.S. Pat. No. 4,994,534.

The polymerization system may comprise a single reactor or two or morereactors in series, and is conducted substantially in the absence ofcatalyst poisons. Organometallic compounds may be employed as scavengingagents for poisons to increase the catalyst activity. Examples ofscavenging agents are metal alkyls, preferably aluminum alkyls.

Conventional adjuvants may be used in the process, provided they do notinterfere with the operation of the catalyst composition in forming thedesired polyolefin. Hydrogen may be used as a chain transfer agent inthe process, in amounts up to about 10 moles of hydrogen per mole oftotal monomer feed.

Polyolefins that may be produced according to the invention include, butare not limited to, those made from olefin monomers such as ethylene andlinear or branched higher alpha-olefin monomers containing 3 to about 20carbon atoms. Homopolymers or interpolymers of ethylene and such higheralpha-olefin monomers, with densities ranging from about 0.86 to about0.97 may be made. Suitable higher alpha-olefin monomers include, forexample, propylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene,1-octene, and 3,5,5-trimethyl-1-hexene. Olefin polymers according to theinvention may also be based on or contain conjugated or non-conjugateddienes, such as linear, branched, or cyclic hydrocarbon dienes havingfrom about 4 to about 20, preferably 4 to 12, carbon atoms. Preferreddienes include 1,4-pentadiene, 1,5-hexadiene, 5-vinyl-2-norbornene,1,7-octadiene, vinyl cyclohexene, dicyclopentadiene, butadiene,isobutylene, isoprene, ethylidene norbornene and the like. Aromaticcompounds having vinyl unsaturation such as styrene and substitutedstyrenes, and polar vinyl monomers such as acrylonitrile, maleic acidesters, vinyl acetate, acrylate esters, methacrylate esters, vinyltrialkyl silanes and the like may be polymerized according to theinvention as well. Specific polyolefins that may be made according tothe invention include, for example, high density polyethylene, mediumdensity polyethylene (including ethylene-butene copolymers andethylene-hexene copolymers) homo-polyethylene, polypropylene,ethylene/propylene rubbers (EPR's), ethylene/propylene/diene terpolymers(EPDM's), polybutadiene, polyisoprene and the like.

Reduced chromium oxide-on-silica catalysts represent one pathway toimproved catalyst systems for polyethylenes having characteristics ofthose typically formed using silylchromate-on-silica catalysts. It isdesired that any such catalytic system exhibit good space-time yield,producing the greatest amount of polyethylene possible with highcatalyst activity. Chromium oxide catalysts possess adequateproductivity and activity, yet polyethylenes produced through their useare less than optimal for a number of applications where high molecularweight, broad molecular weight distribution, and the presence of somedegree of bimodality of molecular weight distribution are desired.

The so-called Phillips catalyst, introduced in the early 1960s was thefirst chromium oxide-on-silica catalyst. The catalyst is formed byimpregnating a Cr⁺³ species into silica, followed by fluidization of thesilica matrix at ca. 400° C.-800° C. Under these conditions, Cr⁺³ isconverted to Cr⁺⁶. The Phillips catalyst is also commonly referred to inthe prior art as “inorganic oxide-supported Cr(+6).” While chromiumoxide-on-silica catalysts exhibit good productivity, they producepolyethylenes having high molecular weight and narrow molecular weightdistribution. The so-called Phillips catalyst and related catalysts areherein referred to as “Oxo-type” catalysts. FIG. 1 gives a schematicrepresentation of the structure of Oxo-type catalysts.Silylchromate-on-silica catalysts are one type of inorganicoxide-supported Cr(+6) catalyst that produces polyethylenes not havingthe aforementioned deficiencies. Silylchromate-on-silica catalysts arereferred to herein as S-type catalysts. FIG. 2 gives a schematicrepresentation of the structure of S-type catalysts. It is and has beena goal to preserve or improve productivity of Oxo-type catalysts, whileproducing a polyethylene with molecular weight and molecular weightdistributions more closely approaching those produced with S-typecatalysts.

Variations on catalysts employing Cr⁺⁶ species supported on silica havebeen known. One particular variation uses titanium tetraisopropoxide(TTIP) impregnated onto silica along with the Cr⁺³ species. Suchmodifications result in polyethylenes with slightly greater molecularweight distributions. While this system produces polyethylenes tendingtowards those produced using silylchromate-on-silica type catalysts,further improvements in molecular weight and molecular weightdistribution more closely approaching those obtained withsilylchromate-on-silica are desired.

Chromium oxide based catalysts have high activity with moderateinduction times. These catalysts make polymer with intermediatemolecular weight distribution. The inventors have found that theaddition of various silanols, in particular, triphenylsilanol, modifiesthe molecular weight distribution of polymers produced with CrOx basedcatalysts. Polymer molecular weight distribution broadens with theformation of a high molecular weight shoulder as determined by sizeexclusion chromatography (SEC). The resulting polymer looks similar to apolymer obtained with silylchromate-based catalysts.

High catalyst activity and broad polymer molecular weight distributionare desired objectives for High Space-Time Yield (HSTY) operation. Assuch, there is a need to produce polymers with characteristics of thoseproduced using silylchromate catalysts, but with higher catalystactivities than those obtained using silylchromate, while maintainingthe polymer molecular weight and performance properties ofsilylchromate-produced polymers.

Additionally, the use of silanols with chromium oxide catalysts areuseful to tuning catalyst activity, polymer molecular weight and thebreadth of the polymer molecular weight distribution by varying theamount of silanol added. Silanol can be used with chromium oxidecatalysts in conjunction with a co-catalyst such as TEA1 or DEALE. Thereagents can be added during a catalyst preparation step (“in catalyst”)or by addition to the reactor separately from the catalyst (“in situ”).The silanols of the present invention can also be used as a replacementfor silylchromate-based catalyst production. Silanols such astriphenylsilanol (TPS) added to chromium oxide-based catalyst can makesimilar catalyst as that made with silylchromate on silica. Oneadvantage of the instant approach is a realization of a reduction ofcatalyst manufacturing costs.

It has also been found that broad molecular weight distributionpolyethylenes can be made in which the comonomer can be incorporatedinto the high molecular weight component by using two chromiumcatalysts. Broad or bimodal molecular weight distribution polyethyleneis especially useful for high environmental stress crack resistant(ESCR) applications such as large part blow molding, or pipe. It hasbeen observed that some chromium oxide catalysts or chromium oxidecatalysts reduced with aluminum alkyls, such as TEA1, are capable ofvery high molecular weight polyethylene with significant comonomerincorporated. When combined with a chromium catalyst that makes a lowermolecular weight polymer with little comonomer incorporation undersimilar conditions, (e.g., silylchromate) or a chromium oxide catalysttreated with DEALE or with a silanol such as TPS plus DEALE, the desiredpolymer can be produced.

Chromium oxide catalysts activated at 600-825° C. with loadings of0.25-0.5 wt. % chromium on Davison 955 silica followed by reduction withTEA1 are particularly useful to make the high molecular weight component(this catalyst component can also be treated with a silanol (e.g., TPS)prior to aluminum alkyl (e.g., TEA1) reduction to also obtain a veryhigh molecular weight polymer). This catalyst still incorporatescomonomer at a high rate and is capable of making comonomer in situ. Thelow molecular weight component can be made with a highly reducedsilylchromate-type catalyst. However, the inventors have found that verylow molecular weight polymer can be made when activated chromium oxidecatalyst is treated with TPS and then DEALE. The broad molecular weightdistribution can be made by blending the polymer components madeindividually by each catalyst system or by first blending the catalystsand then making the mixed polymers during the polymerization reaction.The inventors have found that a very broad molecular weight distributioncan be obtained without an excessive increase in the z-average molecularweight (M_(z)) component. This is particularly important to allow forhigh ESCR without a significant increase in polymer swell.

While in many of the examples that follow, DEALE is used, other aluminumalkyls may be used. Similarly, where DEALE is used, it should beunderstood that other alkyl aluminum alkoxides may be used and where TPSis used, other silanols may be substituted. In general, the alkyl groupsof the aluminum alkyl can be the same or different, and should have fromabout 1 to about 12 carbon atoms and preferably 2 to 4 carbon atoms.Examples include, but are not limited to, triethylaluminum,tri-isopropylaluminum, tri-isobutyl aluminum, tri-n-hexyl aluminum,methyl diethylaluminum, and trimethylaluminum. Although the examplesfocus primarily on the use of TEA1, it should be understood that theinvention is not so limited. In general, the alkyl aluminum alkoxide,having the general formula R₂—Al—OR where the alkyl groups may be thesame or different, should have from about 1 to about 12 carbon atoms andpreferably 2 to 4 carbon atoms. Examples include but are not limited to,diethyl aluminum ethoxide, diethyl aluminum methoxide, dimethyl aluminumethoxide, di-isopropyl aluminum ethoxide, diethyl aluminum propoxide,di-isobutyl aluminum ethoxide, and methyl ethyl aluminum ethoxide.Although the examples almost exclusively use DEALE, it should beunderstood that the invention is not so limited. Additionally withrespect to the silanols useful in the present invention, a number ofsilanols may be used. These include triphenyl silanol, methyl diphenylsilanol, trimethyl silanol, triethyl silanol, triisobutyl silanol, aswell as others.

Table 1 lists several exemplary commercial silica supports with theirphysical properties. These silica supports are illustrative examples andnot exhaustive of the types of silica which may be used in the presentinvention. Other silica supports commonly used in the field and known tothose of skill in the art are also useful herein. Table 1 providesapproximate pore volume, surface area, average pore diameter, averagepore size and percent titanium for the silica supports used in thisstudy. The label is that used by the supplier to describe the support.The number without the parentheses is the name of the support suppliedas silica alone. The number in parentheses is the name of the supportwhen it is supplied with a chromium salt already impregnated on thesupport. Although these silicas were obtained from the suppliers anysilica fitting the specifications below would be expected to function ina similar manner. The present invention is not limited to any specificcommercial silica support but may be used with any silicas having a porevolume of about 1.1-1.8 cm³/g and a surface area of about 245-375 m²/g;or a pore volume of about 2.4-3.7 cm³/g and a surface area of about410-620 m²/g; or a pore volume of about 0.9-1.4 cm³/g and a surface areaof about 390-590 m²/g. TABLE 1 Commercial Silica Supports and PhysicalProperties Average Pore Surface Pore Average Volume Area Diameter PoreSize Silica Support (cm³/g) (m²/g) (Å) (μm) Ti (%) Grace 955 1.45 310210 55 — (957) PQ MS3050 3.02 513 198 90 — (35100) Ineos EP52 1.15 49090 70 2.60 (352)General Catalyst Preparations

Unless otherwise noted the catalysts used in the following examples wereall made by the following procedures.

General Preparation A. Chromium oxide catalyst activation: Catalystswere received from the suppliers with the chromium already impregnatedon the supports. The catalyst physical properties are described inTable 1. Activation is conducted by passing gas through the catalyst forfour hours at the specified temperature in dry air. This is usuallyconducted in a tube furnace. The catalyst is then stored under nitrogenuntil used.

General Preparation B Chromium oxide catalyst treatment: In a typicalpreparation 3 grams of previously activated catalyst is placed in a 50mL airless ware flask with a stir bar under inert atmosphere.Thirty-five mL of dry degassed hexane is added and the mixture is heatedto 50° C. The silanol is then added via syringe. The mixture is stirred2 hours followed by alkylaluminum addition, when used (all reagents are20-25 wt. % in hexane). The stated equivalents are always the ratio ofreagent to chromium. After 30 minutes, drying is commenced. This can bedone under high vacuum or with a nitrogen purge. Catalyst is storedunder n until used.

Catalyst Descriptions

When used, the ratio of reagents to chromium added can be found in theexample; “in reactor” means the catalyst was added separately from thecatalyst. “On catalyst” means the reagent is added in a catalystpreparation step.

EXAMPLE 1

The catalyst was used as supplied by Davison Chemical and consists of0.5 wt. % chromium on Davison 955 silica and was activated at 825° C.(General preparation A). See silica specifications in Table 1.

EXAMPLES 2-3

The catalyst is the same as that used in Example 1 except that TPS isadded in a catalyst preparation step as in General preparation B.

EXAMPLES 4-6

The catalysts are the same as examples 1-3 except the silica containedonly 0.25 wt. % chromium and was activated at 600° C.

EXAMPLES 7-8

The catalyst is the same as that used in example 1 except the catalystwas activated at 600° C.

EXAMPLES 9-10

The catalyst consists of 0.5 wt. % Cr on Davison 955 silica (200° C.dehydration) treated with titanium tetra-isopropoxide prior toactivation. Enough TTIP is added so after activation 3.8 wt. % Tiremains (see U.S. Pat. No. 4,011,382 for specific procedures for TTIPaddition). Activation was done at 825° C. TPS was added in reactor.

EXAMPLES 11-12

Same catalyst as that used in example 9.

EXAMPLES 13-16

Same catalyst as that used in example 1. When used on catalyst TPS andDEALE are added as in General prep B.

EXAMPLES 17-18

The catalyst is the same as that used in example 7.

EXAMPLE 19-22

The catalyst is the same as that used in example 4. When used oncatalyst, TPS and DEALE are added as in General prep B.

EXAMPLES 23-24

The catalyst is the same as that used in example 9.

EXAMPLE 25

The catalyst is the same as that used in example 1 treated with TPS andtriisobutyl aluminum (TIBA) as in General prep B.

EXAMPLES 26-29

The catalyst is the same as that used in example 1. When used, DEALSi isadded to the reactor separately. DEALSi is formed by mixing in hexaneequal molar amounts of triethylsilanol and triethylaluminum.

EXAMPLES 30-32

The catalyst is the same as that used in example 9. When used, DEALSi isadded to the reactor separately.

EXAMPLES 33-35

The catalyst used is MS35100 which is a chromium oxide catalyst on MS3050 silica obtained from PQ with the specifications listed in Table 1.The catalyst contains 0.5 wt. % Cr. The catalyst is activated at 700° C.(General preparation A). When used on catalyst, TPS and DEALE are addedas in General prep B.

EXAMPLE 36

The catalyst is the same as that used in example 4 treated with 2equivalents of TEA1 as in General prep B.

EXAMPLE 37

The catalyst is the same as that used in example 7 treated with TPS andDEALE as in General prep. B.

EXAMPLE 38

Equal weight amounts of the catalysts from examples 36 and 37 are usedhere.

EXAMPLE 39

Catalyst preparation: 3.59 grams of previously dehydrated 955 silica isplaced in a 50 mL airless ware flask with a stir bar under inertatmosphere. Next 0.112 grams of bis-triphenylsilyl chromate is added.Thirty-five mL of dry degassed hexane is added and the mixture is heatedto 50° C. The mixture is stirred for 2 hours, then 10 equivalents ofDEALE is added. After 30 minutes at 50° C., the mixture is dried underhigh vacuum.

Lab Slurry Procedure

A one liter stirred reactor was used for the polymerization reactions.The reactor was thoroughly dried under a purge of nitrogen at elevatedtemperatures before each run. 500 mL of dry degassed hexane was fed tothe reactor at 60° C. If used, hexene is added at this point. Unlessotherwise noted 10 mL of 1-hexene is used in each experiment. A smallquantity (0.1-0.25 g) of Davison 955 silica dehydrated at 600° C. andtreated with 0.6 mmole/g of TEA1 is then added to the reactor topassivate any impurities. No TEA1 treated silica was added in any runwhere a reagent was added to the reactor separately from the catalyst.After stirring for 15 minutes the catalyst is charged followed byadditional reagents. When silanols and alkylaluminum reagents are addedseparately to the reactor from the catalyst, the silanol is added firstfollowed by the addition of the alkylaluminum. Both are added as dilutehexane solutions. The reactor is sealed and hydrogen is charged at thispoint. Hydrogen is only used where noted in the tables. The reactor ischarged to 200 psi with ethylene. Ethylene is allowed to flow tomaintain the reactor pressure at 200 psi. Ethylene uptake is measurewith an electronic flow meter. All copolymerizations were run at 85° C.Polymerizations were run until a maximum of 160 grams polyethylene weremade or terminated sooner. The reactor was opened after depressurizationand the temperature lowered. The polymer weight was determined afterallowing the diluent to evaporate. The polymer was then characterizedemploying a number of tests.

Tests

Density: ASTM D-1505.

Melt Index: (12) ASTM D-2338 Condition E measured at 190° C. reported asgrams per 10 minutes.

Flow Index: (I₂₁) ASTM D-1238 Condition F measured at 190° C. using 10times the weight as used in Melt Index above.

MFR: Melt Flow ratio is the Flow index/Melt index.

SEC: Polymer Laboratories instrument; Model: HT-GPC-220, Columns:Shodex, Run Temp: 140° C., Calibration Standard: traceable to NIST,Solvent: 1,2,4-Trichlorobenzene. Mn and Mw values in the tables shouldbe multiplied by 10³. Mz values multiplied by 10⁶.

BBF: Butyl branching frequency as measured by ¹³C-NMR. The value is thenumber of butyl branches per 1000 carbon atoms.

Effect of Silanol on CrOx Catalyst: Molecular Weight Distribution,Molecular Weight, and Productivity

The effect of adding arylsilanol to chromium oxide catalyst systems wasstudied using chromium oxide (0.5 wt. %) loaded onto 955-type silicaactivated at 825° C. (see Table 2, examples 1-3), having a pore volumeof about 1.1-1.8 cm³/g and a surface area of about 245-375 m²/g. TPS wasused as the arylsilanol in this example. A clear trend in broadeningmolecular weight distribution (Mw/Mn) is seen when 2 equivalents of TPSare added, relative to that seen for 1 equivalent of TPS and in theabsence of TPS. An increase in M_(Z)/M_(W) indicates the growth of ahigh molecular weight shoulder as TPS is added. Polymer density wasobserved to increase when TPS was added indicating lower comonomerincorporation. Desired densities of about 0.918-0.970 g/cm³, amongothers, of the resulting polymers may be so obtained. BBF measurementsconfirm lower comonomer incorporation (see Table 2). Polymer molecularweight also increases. Catalyst activity is found to decrease as theamount of TPS is increased. Lower catalyst activity is due to acombination of longer induction times and lower inherent activity (FIG.3). TABLE 2 Effect of Triphenyl Silanol (TPS) on Oxo Chromium CatalystBulk TPS added Time YIELD Flow Act. gPE/ Density to catalyst (min) (g)Index gcat-1 hr (g/cc) CrOx on 955 Silica/0.5 wt % Examples Cr; 825 C.activation Mn Mw Mz Mw/Mn Mz/Mw BBF 1 none 58 153 2.6 1,429 0.34 25.1243 1.09 9.68 4.47 3.7 2 1 eq. 80 161 2.1 607 0.42 21.4 283 1.46 13.265.17 2.9 3 2 eq. 160 101 2.6 102 0.35 10.3 348 2.16 33.90 6.22 1.9

FIG. 4 illustrates the molecular weight plots (data obtained by SEC) forpolymers made with CrOx with no TPS (FIG. 4 a); CrOx with 1 equivalentof TPS (FIG. 4 b); and CrOx with 2 equivalents of TPS (FIG. 4 c)(examples 1-30). The high molecular weight shoulder becomes pronouncedfor polymer produced with CrOx catalyst in the presence of 2 equivalentsof TPS. Although not readily apparent from the figures, the highmolecular weight shoulder also increases in magnitude in going frompolymer produced in the absence of TPS to that produced in the presenceof 1 equivalent of TPS. This trend is evidenced by the increase inM_(z)/M_(w) values of 4.47 and 5.17, respectively for polymer producedwith CrOx in the absence of TPS and that produced with CrOx in thepresence of 1 equivalent of TPS. Polymer MWD can be varied bycontrolling the amount of arylsilanol added to the catalyst. TABLE 3Effect of Triphenyl Silanol (TPS) on Oxo Chromium Catalyst Catalyst andTPS Time YIELD Act. gPE/ Den. Examples addition method (min) (g) FIgcat-1 hr BD Mn Mw Mz Mw/Mn Mz/Mw g/cc CrOx on 955 Silica/0.25 wt % Cr;600 C. activation  4* no TPS 72 174 1.1 765 0.28 18.1 356 1.79 20 5.00.9360 5 1 eq. TPS on 118 143 1.1 274 0.35 15.6 409 1.92 26 4.7 0.9423catalyst 6 2 eq. TPS on 300 78 3.8 30 0.26 11.6 327 1.68 28 5.1 0.9447catalyst CrOx on 955 Silica/0.50 wt % Cr; 600 C. activation 7 no TPS 110154 5.6 1,074 0.32 14.9 294 1.54 20 5.2 0.9402 8 1 eq. TPS in 94 179 1.0472 0.32 15.6 368 1.71 24 4.7 0.9407 reactor TiCrOx on 955 Silica/0.5 wt% Cr; 825 C. activation 9 no TPS 62 156 3.8 1,497 0.32 12.6 212 0.88 174.2 0.9466 10  1 eq. TPS in 65 161 6.1 612 0.29 10.1 234 1.27 23 5.40.9470 reactor[*20 ml 1-hexene used here]

In Table 3 (examples 4-6), data is presented for CrOx on 955-type silicaat a loading of 0.25 wt. % chromium and activated at 600° C. in theabsence of TPS; in the presence of 1 equivalent of TPS; and in thepresence of 2 equivalents of TPS. Also shown is data for CrOx on955-type silica at a loading of 0.5 wt. % chromium and activated at 600°C. in the absence of TPS and in the presence of 1 equivalent of TPSadded in situ. Finally, there is data for titanated chromium oxide on955-type silica activated at 825° C. in the absence of TPS and with 1equivalent of TPS added in situ. The effect of TPS is apparent.Molecular weight distribution broadens but without a significantincrease in the high molecular weight tail. In examples 4-10 thecatalyst induction periods were observed to increase when TPS is added(FIG. 5). FIG. 5(a) shows chromium oxide on 955-type silica activated at600° C.; FIG. 5(b) shows titanated chromium oxide on 955-type silicaactivated at 825° C.

In comparison with the above-presented data, it can be seen that themolecular weight effects are catalyst-specific. In the present example,molecular weight distribution is broadened, but the high molecularweight shoulder was not enhanced; in the earlier example, the additionof TPS both broadened the molecular weight distribution and increasedthe intensity of the high molecular weight shoulder.

In Table 4 (examples 11-14), data is presented for triethylsilanol (TES)addition to chromium oxide catalysts in ethylene polymerizationreactions. Separate addition of TES to polymerization reactionscatalyzed with titanated chromium oxide on 955 type silica and chromiumoxide on 955 type silica, both with 0.5 wt. % chromium and activated at825° C., led to much reduced activity and little or no change in polymermolecular weight distribution. In FIG. 6 it can be seen that TESaddition leads to longer induction periods and lower activity levels.This shows that not only is this technology catalyst specific, it isalso silanol specific. TABLE 4 Addition of TES to Chromium Oxo CatalystsCatalyst and TEX Time YIELD Act. gPE/ Act. gPE/ Mn Mw Mz Den. Examplesaddition method (min) (g) FI gcat-1 hr gcat-1 hr (×10³) (×10³) (×10⁶)Mw/Mn Mz/Mw g/cc TiCrOx on 955 Silica/0.5 wt % Cr; 825 C. activation 11no TES 67 165 12.2 1,309 0.23 9.4 170 0.75 18 4.4 0.9403 12 1 eq. TES in97 162 7.7 386 0.27 12.7 231 1.27 18 5.5 0.9469 reactor CrOx on 955Silica/0.5 wt % Cr; 825 C. activation 13 no TES 59 101164 3.8 1,416 0.2822.7 271 1.38 12 5.1 0.9399 14 1 eq. TES in 110 160 2.1 338 0.28 22.1302 1.52 14 5.0 0.9398 reactor

Alkyl silanols also provide for useful chemistry when alkyl aluminumalkoxides are used with CrOx-type catalysts. The addition of silanolsand alkyl aluminum alkoxides can be used to convert CrOx catalysts andtitanated CrOx catalysts into catalyst systems providing performancesimilar to silylchromate-based catalyst systems. Silylchromate-basedcatalysts generally produce desirable polyethylenes relative to thoseproduced by chromium oxide-type catalysts. Silylchromate producedpolyethylenes generally have a broader molecular weight distributionthan those produced using chromium oxide-type catalysts. The broadermolecular weight distribution leads to better processability of theresulting polyethylene. However, the productivities ofsilylchromate-based catalysts are typically much poorer than thoserealized using chromium oxide-based catalysts. TABLE 5 Effect of TPS andAlkylaluminum Compounds of Chromium Oxo Catalysts Catalyst and modifiersH2 Time YIELD Act. gPE/ Den. Examples addition method (scc) (min) (g) FIgcat-1 hr BD Mn Mw Mz DI Z/W g/cc CrOx on 955 Silica/0.5 wt % Cr; 825 C.activation 15 none 0 79 174 2.4 1,250 0.32 26.4 268 1.33 10.1 5.0 0.942516 1 eq. TPS + 5 eq. 0 49 126 47.5 1,523 0.30 10.7 197 2.03 18.5 10.30.9622 DEALE in catalyst CrOx on 955 Silica/0.5 wt % Cr; 600 C.activation 17 none 500 110 154 5.6 1,074 0.32 14.9 294 1.54 20.0 5.20.9402 18 1 eq. TPS + 5 eq. 500 116 120 14.8 490 0.33 13.8 278 1.93 20.16.9 0.9583 DEALE in reactor CrOx on 955 Silica/0.25 wt % Cr; 600 C.activation  19* none 500 72 174 1.1 765 0.28 18.1 356 1.79 19.6 5.00.9360 20 1 eq. TPS + 5 eq. 500 71 154 38.7 590 0.37 8.3 192 2.00 23.210.4 0.9595 DEALE in reactor 21 2 eq. TPS + 5 eq. 500 78 156 29.5 3090.41 7.8 212 1.88 27.3 8.9 0.9594 DEALE in reactor 22 1 eq. TPS + 5 eq.500 34 153 148.1 1,211 0.38 DEALE in catalyst TiCrOx on 955 Silica/0.5wt % Cr; 825 C. activation 23 none 500 64 175 9.7 1,380 0.32 9.8 1820.81 18.5 4.47 0.9471 24 1 eq. TPS + 5 eq. 500 72 176 42.2 703 0.29 7.8196 1.66 25.0 8.47 0.9599 DEALE in reactor CrOx on 955 Silica/0.5 wt %Cr; 825 C. activation 25 1 eq. TPS + 5 eq. 500 72 145 5.4 496 0.310.9501 TIBA in catalyst[*20 ml 1-hexene used here]

Table 5 illustrates the effect of the addition of silanol and alkylaluminum alkoxide to chromium oxide-based catalyst on 955-type silica.Polymerizations without silanol or any organoaluminum is compared withanalogous systems having 5 equivalents of DEALE and 1 equivalent of TPSadded to the catalyst. (0.5 wt. % of chromium loading and activated at825° C.; examples 15 and 16). Significant increase in polymer flow indexand polymer molecular weight distribution accompanied by a highmolecular weight shoulder (very high Mz/Mw) can be seen. Addition ofalkyl aluminum alkoxide and alkyl silanol can be used to control theseparameters. Although values outside this range are attainable, desirableflow index values from about 1-500 can be achieved. Catalyst activity isalso observed to increase and catalyst induction period normallyassociated with TPS addition is eliminated. The combination of the TPSand DEALE produce the desired polymer molecular weight distributionwhile decreasing catalyst induction time compared to that found withoutDEALE addition (FIG. 7). The same comparison can be seen in Examples 17and 18 except that the catalyst activation was conducted at 600° C. andthe TPS and DEALE were added to the reactor. The polymer molecularweight drops, the molecular weight distribution remains the same but thehigh molecular weight shoulder is seen to increase. In examples 19 to22, the same catalyst is used as in the previous examples except thatthe chromium loading is 0.25 wt. %. When TPS and DEALE are added to thereactor (examples 20 and 21), the polymer molecular weight is observedto decrease, molecular weight distribution increases and the highmolecular weight shoulder increases (higher Mz/Mw) compared to theunmodified catalyst. When the components were added to the catalyst(example 22), higher catalyst activity and polymer flow index valueswere found. Utility lies in the ability to control these parameters,allowing one a greater ability to tailor the characteristics of thepolymer produced.

In Example 24 separate addition of TPS and DEALE to a polymerizationreaction using titanated chromium oxide catalyst (0.5 wt. % Cr) on 955type silica activated at 825° C. was conducted. In comparison to thesame reaction without TPS and DEALE (example 23), polymer molecular flowindex is observed to increase, molecular distribution increases and thehigh molecular weight shoulder increases (higher Mz/Mw).

In Example 25 it can be seen that other alkyl aluminum reagents can beused in conjunction with chromium oxide catalysts and TPS. In thisexample, the same catalyst is used as in example 16 is used except thattriisobutyl aluminum (TIBA) is used in place of DEALE. When TIBA is usedin place of DEALE higher molecular weight polymers are obtained.

Although the specific silica supported chromium oxide catalyst mayaffect results, it can be seen that when alkyl aluminum or alkylaluminum alkoxides are used with TPS, lower molecular weight polymerswith broader molecular weight distributions and increased high molecularweight shoulders can be obtained without unacceptable losses in catalystactivity due to long induction times and lower activities as found withTPS and chromium oxide catalysts alone. Polymer molecular weights aretoo high for most product applications in the absence of alkyl aluminumand alkyl aluminum alkoxides.

The addition of diethylaluminum triethylsiloxide (DEALSi) to chromiumoxide or titanated chromium oxide catalyst yields results similar tothose obtained using silylchromate-based catalysts. Generally, higherproductivities for the catalysts, and higher molecular weights for theresulting polyethylenes are obtained when using chromium oxide ortitanated chromium oxide catalyst in the presence of DEALSi. DEALSi isthe reaction product of one equivalent each of triethyl silanol andtriethyl aluminum. As DEALSi is added spanning the range of 2 to 5 and10 equivalents, an increase in polymer flow index is observed. (Table 6,examples 26 through 32). Induction time is altered and the kineticprofile shows an elimination of induction time in the presence of DEALSi(see FIG. 8). Additionally, the data in Table 6 shows that polyethyleneshaving broader molecular weight distribution and a more pronounced highmolecular weight shoulder result from the introduction of DEALSi intochromium oxide-based catalyst systems. Addition of TES alone to chromeoxide catalysts as shown in Table 4 did not modify polymer propertiesand significantly poisoned the catalysts. The reaction product of TEA1and TES in conjunction with specific catalysts allows for high catalystactivities, improved flow index response and polymer molecular weightdistribution. TABLE 6 Effect of DEALSi on Chromium Oxo Catalysts DEALSiin Time YIELD Flow Act. gPE/ Den. Examples situ addition (min) (g) Indexgcat-1 hr BD Mn Mw Mz DI Z/W g/cc CrOx on 955 Silica/0.5 wt % Cr; 825 C.activation 26 none 59 164 3.8 1,416 0.28 22.7 271 1.38 12.0 5.07 0.939927 2 eq. 56 151 29.9 1,101 0.33 0.9554 28 5 eq. 55 147 34.4 1,027 0.3510.7 160 1.46 15.0 9.13 0.9540 29 10 eq. 63 141 42.3 975 0.33 0.9562TiCrOx on 955 Silica/0.5 wt % Cr; 825 C. activation  30* none 67 16512.2 1,309 0.23 9.4 170 0.75 18.0 4.42 0.9403 31 2 eq. 80 169 34.4 8380.35 0.9558 32 5 eq. 68 143 21.5 814 0.32 8.5 170 1.38 20.1 8.08 0.9564[*20 ml 1-hexene used here]

Table 7 illustrates the effect of the addition of silanol and alkylaluminum alkoxide to chromium oxide-based catalyst on MS 3050-typesilica (0.5 wt. % of chromium loading and activated at 700° C.).Addition of TPS and DEALE either in the reactor or on the catalystresults in increased activity and a lowering of polymer molecular weight(examples 34 and 35). Polymer molecular weight distribution did notchange but the high molecular shoulder increased significantly based onMz/Mw values. The activity increased due to elimination of the inductionperiod. Without TPS and DEALE addition this catalyst produces polymerwith very low flow index indicative of unacceptably high polymermolecular weight (examples 33).

The results in Table 7 show that more than one kind of silica respondsin the same manner to addition of silanols and alkylaluminum alkoxides.TABLE 7 Effect of TPS and Alkyl Aluminum Compounds on Chromium OxoCatalyst on MS 3050 Silica Catalyst and modifiers H2 Time additionmethod (scc) (min) CrOx on MS3050 silica/0.5 wt % YIELD Act. gPE/ Den.Examples Cr; 700 C. activation (g) FI gcat-1 hr BD Mn Mw Mz DI Z/W g/cc33 none 500 82 212 1.4 695 0.35 20.9 452 2.27 21.60 5.01 0.9411 34 1 eq.TPS + 5 eq. 500 54 188 38.0 864 0.35 10.2 190 1.81 18.50 9.56 0.9585DEALE in reactor 35 1 eq. TPS + 5 eq. 500 32 179 64.7 1,978 0.38 0.9613DEALE in catalyst[* 20 ml 1-hexene used here]Effect of Silanol on Bimodality of Molecular Weight Distribution.

The molecular weight manipulations made possible by the presentinvention can be extended through the use of dual chromium-basedcatalysts to increase the level of bimodality in the resultingpolyethylene. It is desirable to produce a high density polyethylene inwhich the side chain branching is primarily found only in the highmolecular weight shoulder component of the polymer. This is achievedthrough the use of a dual catalyst system employing two chromium basedcatalysts. In one example, there is a catalyst based on chromium oxideon silica or chromium oxide on silica that can be reduced with atrialkyl aluminum compound such as TEA1. The second catalyst is chromiumoxide treated with TPS and DEALE. Table 8 provides results forpolyethylenes produced with each catalyst separately and with this dualcatalyst system all under the same reaction conditions. The use of aTEA1 reduced chromium oxide catalyst on 955 silica and activated at 600°C. (example 36) resulted in the formation of polymer with very highmolecular weight (Mw>390,000). The density shows that a significant ofcomonomer was incorporated in the polymer. The use of chromium oxidecatalyst on 955 silica and activated at 600° C. followed by treatmentwith TPS and DEALE (example 37) results in formation of polymer withvery low molecular weight (Mw<115,000). The polymer density is very highapproaching homopolymer levels indicating little or none comonomer wasincorporated into the polymer. Employment of equal amounts of eachcatalyst (example 38) resulted in formation of a polymer withintermediate molecular weight and density, but with broader molecularweight distributions. This shows that both catalysts were active andthat the high molecular weight portion of the polymer would contain thecomonomer. In example 39 is seen another catalyst capable of producinglow molecular weight polymer with low comonomer incorporation rates.This silylchromate based catalyst that has been reduced with high levelof DEALE can be used in conjunction with the chromium oxide catalystsdescribed above that make the high molecular weight, high comonomercontaining component. TABLE 8 Dual Chromium Catalyst System for BimodalHDPE Catalyst Time YIELD Flow Act. gPE/ Mw Mz Den. Examples Catalystmodification (min) (g) Index gcat-1 hr BD Mn Mw Mz Mn Mw g/cc IndividualCatalyst Components 36 CrOx on 955 2 eq. TEAI 47 166 0.6 865 0.35 17.5393 1.76 22.4 4.5 0.9430 Silica/0.25 wt % Cr; 600 C. activation 37 CrOxon 955 1 eq. TPS 36 153 205.5 1,028 0.40 6.8 114 1.21 16.8 10.5 0.9623Silica/0.5 wt % Cr; 2 eq. DEALE 600 C. activation Catalyst Blend 38 1:1ratio of 69 163 7.1 659 0.34 8.9 292 1.56 33.0 5.3 0.9509 cataly stsfromexamples 32 and 33 39 Silychromate 10 eq. DEALE 47 155 87.0 788 0.360.9638 (0.24 wt. %) on 955 on catalyst silica dehydrated at 600 C.

The dual catalyst system produces a polyethylene having a very broadmolecular weight distribution with comonomer incorporation in higherconcentration in the high molecular weight region of the distribution.Polymer made with the dual catalyst system would be expected to haveimproved ESCR properties as well as improved pipe properties.

Although the present invention and its advantages have been described indetail, it should be understood that various changes, substitutions andalterations can be made herein without departing from the spirit andscope of the invention as defined by the appended claims. Moreover, thescope of the present application is not intended to be limited to theparticular embodiments of the process, machine, manufacture, compositionof matter, means, methods and steps described in the specification. Asone of ordinary skill in the art will readily appreciate from thedisclosure of the present invention, processes, machines, manufacture,compositions of matter, means, methods, or steps, presently existing orlater to be developed that perform substantially the same function orachieve substantially the same result as the corresponding embodimentsdescribed herein may be utilized according to the present invention.Accordingly, the appended claims are intended to include within theirscope such processes, machines, manufacture, compositions of matter,means, methods, or steps.

1. A supported chromium catalyst comprising: chromium oxide, asilica-containing support comprising silica selected from the groupconsisting of silica having: (a) a pore volume of about 1.1-1.8 cm³/gand a surface area of about 245-375 m²/g; (b) a pore volume of about2.4-3.7 cm³/g and a surface area of about 410-620 m²/g; and (c) a porevolume of about 0.9-1.4 cm³/g and a surface area of about 390-590 m²/g;and, an alkyl silanol, wherein said supported chromium catalyst isactivated at 400-860° C., prior to the addition of said alkyl silanol.2. The catalyst of claim 1 further comprising an organoaluminumcompound.
 3. The catalyst of claim 2 wherein said activated chromiumcatalyst is treated first with said alkyl silanol and then with saidorganoaluminum compound.
 4. The catalyst of claim 2 wherein said silicahas a pore volume of about 2.4-3.7 cm³/g and a surface area of about410-620 m²/g and said organoaluminum compound is an alkyl aluminumalkoxide compound.
 5. The catalyst of claim 2 wherein said silica has apore volume of about 1.1-1.8 cm³/g and a surface area of about 245-375m²/g, and said organoaluminum compound is an alkyl aluminum alkoxidecompound.
 6. The catalyst of claim 2 wherein said organoaluminumcompound is added in-situ.
 7. The catalyst of claim 2 further comprisingat least a second chromium-based compound.
 8. The catalyst of claim 7wherein said second chromium-based compound is a chromium oxide onsilica or an organoaluminum-reduced chromium oxide on silica.
 9. Thecatalyst of claim 2 wherein said alkyl silanol or said organoaluminumcompound or both said alkyl silanol and said organoaluminum compound areadded in-situ.
 10. The catalyst of claim 9 wherein said alkyl silanoland said organoaluminum compound are pre-mixed prior to said in-situaddition.
 11. The catalyst of claim 2 wherein said organoaluminumcompound is an alkyl aluminum alkoxide compound.
 12. The catalyst ofclaim 11 wherein said alkyl aluminum alkoxide compound is diethylaluminum ethoxide.
 13. The catalyst of claim 11 formed by the in situaddition of said alkyl aluminum alkoxide compound.
 14. The catalyst ofclaim 13 wherein said alkyl aluminum alkoxide compound is diethylaluminum ethoxide.
 15. The catalyst of claim 2 wherein saidorganoaluminum compound is an alkyl aluminum compound.
 16. The catalystof claim 15 wherein said alkyl aluminum compound is selected from thegroup consisting of triethyl aluminum, tri-isobutyl aluminum, andtri-n-hexyl aluminum.
 17. The catalyst of claim 16 formed by the in situaddition of said alkyl aluminum compound.
 18. The catalyst of claim 16wherein said alkyl aluminum compound is tri-isobutyl aluminum.
 19. Thecatalyst of claim 1 wherein said supported chromium catalyst isactivated at 600-860° C.
 20. The catalyst of claim 1 wherein said alkylsilanol is triphenyl silanol.
 21. A process for producing an ethylenepolymer comprising the steps of: contacting ethylene underpolymerization conditions with a catalyst system, said catalyst systemcomprising chromium oxide, an alkyl silanol compound, and asilica-containing support comprising silica selected from the groupconsisting of silica having: (a) a pore volume of about 1.1-1.8 cm³/gand a surface area of about 245-375 m²/g; (b) a pore volume of about2.4-3.7 cm³/g and a surface area of about 410-620 m²/g; and (c) a porevolume of about 0.9-1.4 cm³/g and a surface area of about 390-590 m²/g;and, controlling one or more of catalyst activity, polymer Mz/Mw,polymer Mw/Mn, and polymer density of the resulting ethylene polymer byvarying the level of addition of said alkyl silanol.
 22. The process ofclaim 21 wherein said polymer Mw/Mn is controlled to greater than about15 and said polymer Mz/Mw is controlled to greater than about
 5. 23. Theprocess of claim 21 wherein said catalyst system further comprises anorganoaluminum compound.
 24. The process of claim 23 wherein saidcatalyst system further comprises at least a second chromium-basedcatalyst.
 25. The process of claim 24 wherein said second chromium-basedcompound is a chromium oxide on silica or an organoaluminum-reducedchromium oxide on silica.
 26. The process of claim 23 wherein saidorganoaluminum compound is an alkyl aluminum alkoxide.
 27. The processof claim 26 wherein said alkyl aluminum alkoxide comprisesdiethylaluminum ethoxide.
 28. The process of claim 23 wherein saidorganoaluminum compound is an alkyl aluminum compound.
 29. The processof claim 28 wherein said alkyl aluminum compound is selected from thegroup consisting of triethyl aluminum, tri-isobutyl aluminum, andtri-n-hexyl aluminum.
 30. The process of claim 21, wherein said processis a gas phase process.